Variant #0000178786 (NC_000004.11:g.73179445C>T, NM_014243.2:c.1694G>A (ADAMTS3))
Chromosome |
4 |
Allele |
Paternal (inferred) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.73179445C>T |
DNA change (hg38) |
g.72313728C>T |
Published as |
R565Q |
ISCN |
- |
DB-ID |
ADAMTS3_000003 See all 3 reported entries |
Variant remarks |
- |
Reference |
PubMed: Jha et al., 2017 |
ClinVar ID |
- |
dbSNP ID |
rs141374503 |
Origin |
Germline |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00215 View details |
Owner |
Pascal Brouillard |
Database submission license |
No license selected |
Created by |
Pascal Brouillard |
Date created |
2017-08-01 10:25:04 +02:00 (CEST) |
Date last edited |
2020-03-29 12:37:28 +02:00 (CEST) |

Variant on transcripts
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